Voltammetry of Ion Transfer at a Water-Toluene Micro-Interface

被引:13
|
作者
Kasuno, Megumi [1 ]
Matsuyama, Yuki [1 ]
Iijima, Misaki [1 ]
机构
[1] Ryukoku Univ, Dept Chem Mat, Otsu, Shiga 5202194, Japan
来源
CHEMELECTROCHEM | 2016年 / 3卷 / 05期
关键词
charge transfer; formal potential; micro-interfaces; toluene; voltammetry; STANDARD GIBBS ENERGIES; OCTYL ETHER INTERFACE; LIQUID/LIQUID INTERFACE; LIQUID; ELECTROCHEMISTRY; SOLVENTS; ELECTROLYTE; FILMS;
D O I
10.1002/celc.201500568
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Voltammograms of ion transfer at the water (W)vertical bar toluene interface were recorded for the first time by using a micro-interface electrolytic cell and bis(triphenylphosphoranylidene) ammonium tetrakis[3,5-bis(trifluoromethyl) phenyl] borate (BTPPA(+) TFPB-). The high solubility of BTPPA(+)TFPB(-) in toluene at room temperature enabled the electrochemical measurements. The potential window at the Wjtoluene interface is about 1.09 V, which is 0.30 V larger than that at the W vertical bar 1,2-dichloroethane interface when using 10 mmol dm(-3) NaCl as the supporting electrolyte in W. The transfer reactions of quaternary ammonium ions across the Wjtoluene interface were found to be reversible. Formal potentials for ion transfer from W vertical bar to toluene were evaluated, and linear correlations were observed between these formal potentials and the standard potentials reported at the Wjnitrobenzene, W vertical bar 1,2-dichloroethane, and W vertical bar 2-nitrophenyl octyl ether interfaces.
引用
收藏
页码:694 / 697
页数:4
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